Total synthesis of malagashanine: a chloroquine potentiating indole alkaloid with unusual stereochemistry
The first total synthesis of malagashanine, a chloroquine potentiating indole alkaloid, is presented. A highly stereoselective cascade annulation reaction was developed to generate the tetracyclic core of the Malagasy alkaloids. This chemistry is likely to be broadly applicable to the synthesis of o...
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Veröffentlicht in: | Chemical science (Cambridge) 2017-01, Vol.8 (1), p.697-700 |
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Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | The first total synthesis of malagashanine, a chloroquine potentiating indole alkaloid, is presented. A highly stereoselective cascade annulation reaction was developed to generate the tetracyclic core of the Malagasy alkaloids. This chemistry is likely to be broadly applicable to the synthesis of other members of this stereochemically unique family of natural products. |
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ISSN: | 2041-6520 2041-6539 |
DOI: | 10.1039/c6sc03578g |